Stearoyl-CoA 9-desaturase
(Redirected from Stearoyl-CoA desaturase-1)
Enzyme involved in fatty acid metabolism
Stearoyl-CoA 9-desaturase (SCD) is an enzyme that plays a crucial role in the metabolism of fatty acids. It is responsible for the introduction of a double bond into saturated fatty acyl-CoA substrates, converting them into monounsaturated fatty acids. This enzyme is particularly important in the biosynthesis of oleic acid from stearic acid.
Function
Stearoyl-CoA 9-desaturase catalyzes the desaturation of stearoyl-CoA to oleoyl-CoA. This reaction involves the insertion of a cis double bond between the ninth and tenth carbon atoms of the fatty acid chain. The enzyme is a member of the fatty acid desaturase family and is located in the endoplasmic reticulum of cells.
The activity of SCD is essential for maintaining the fluidity of cellular membranes and for the production of signaling molecules. The monounsaturated fatty acids produced by SCD are also important precursors for the synthesis of complex lipids such as phospholipids and triglycerides.
Structure
Stearoyl-CoA 9-desaturase is a membrane-bound enzyme that contains several transmembrane domains. It is a diiron enzyme, meaning it contains two iron atoms that are essential for its catalytic activity. These iron atoms are coordinated by histidine residues and are involved in the electron transfer necessary for the desaturation process.
The enzyme's active site is located within the membrane, where it interacts with its fatty acyl-CoA substrate. The crystal structure of SCD has provided insights into its mechanism of action and the arrangement of its active site.
Regulation
The expression and activity of stearoyl-CoA 9-desaturase are tightly regulated by nutritional and hormonal signals. Insulin and dietary carbohydrates can upregulate SCD expression, while polyunsaturated fatty acids and leptin can downregulate it. This regulation is crucial for maintaining lipid homeostasis and energy balance in the body.
Clinical Significance
Alterations in SCD activity have been associated with various metabolic disorders, including obesity, diabetes, and cardiovascular diseases. Increased SCD activity can lead to an accumulation of monounsaturated fatty acids, which may contribute to the development of insulin resistance and other metabolic abnormalities.
Research into SCD inhibitors is ongoing, as these could potentially serve as therapeutic agents for treating metabolic diseases by modulating lipid metabolism.
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Contributors: Prab R. Tumpati, MD